RECRUITING

Can PLIA Reduce Early Post-operative Pain After PAO Surgery?

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to compare different peri-incisional local infiltrative anesthesia (PLIA) methods in patients ages 13 to 50 undergoing a periacetabular osteotomy (PAO). The main questions to answer here are: 1. Does PLIA impact post-operative pain after PAO? 2. Does PLIA impact pain medication usage as measured by morphine equivalent dosing (MED) after PAO? 3. Does the timing of PLIA administration impact post-operative pain and MED after PAO? Participants will be asked to complete some surveys; demographics survey, General Self-Efficacy Scale (GSE) and the Pain Resilience Scale. All other information will be gathered from the patients medical chart. Researchers will compare three groups. 1.) Patients who do not receive PLIA. 2.) Patients who receive PLIA after their incision is closed. 3.) Patients who receive PLIA throughout PAO.

Official Title

Peri-incisional Local Infiltration to Improve Pain Control After Periacetabular Osteotomy

Quick Facts

Study Start:2024-10-03
Study Completion:2026-09
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06519955

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:13 Years to 50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adolescent or young adult diagnosed with hip dysplasia indicated for PAO at University of Iowa Hospital and Clinics.
  1. * Unable to provide informed consent.
  2. * Pregnant or breast-feeding individuals
  3. * Prisoner or ward of the state
  4. * Allergy or medical contradiction to any of the study medications
  5. * Patients undergoing femoral osteotomy or surgical hip dislocation with PAO will be excluded

Contacts and Locations

Study Contact

Ashley S Kochuyt
CONTACT
319-384-5101
ashley-kochuyt@uiowa.edu

Study Locations (Sites)

University of Iowa Health Care
Iowa City, Iowa, 52242
United States

Collaborators and Investigators

Sponsor: Michael C Willey

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-10-03
Study Completion Date2026-09

Study Record Updates

Study Start Date2024-10-03
Study Completion Date2026-09

Terms related to this study

Keywords Provided by Researchers

  • Hip Dysplasia
  • Periacetabular Osteotomy
  • PLIA
  • Peri-Incisional Local Infiltrative Anesthesia

Additional Relevant MeSH Terms

  • Hip Dysplasia